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DIMETHYL 2-[2-(4-METHOXYPHENYL)HYDRAZONO]-3-OXOPENTANEDIOATE is a complex organic chemical compound characterized by the presence of a methoxyphenyl group, a hydrazone group, and an oxopentanedioate group. Although its specific properties and applications are not extensively documented, the compound's general structure suggests potential use in specialized chemical reactions or processes, likely within a laboratory environment.

121582-52-3

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121582-52-3 Usage

Uses

Used in Chemical Research:
DIMETHYL 2-[2-(4-METHOXYPHENYL)HYDRAZONO]-3-OXOPENTANEDIOATE is used as a research compound for exploring its chemical properties and potential applications in organic chemistry. Its unique structure may offer insights into new reaction pathways or mechanisms.
Used in Laboratory Settings:
In a laboratory context, DIMETHYL 2-[2-(4-METHOXYPHENYL)HYDRAZONO]-3-OXOPENTANEDIOATE is used as a reagent or intermediate in specific chemical reactions, potentially leading to the synthesis of new compounds or materials.
Used in Material Science:
DIMETHYL 2-[2-(4-METHOXYPHENYL)HYDRAZONO]-3-OXOPENTANEDIOATE may also find use in material science applications, where its structural components could contribute to the development of novel materials with unique properties.

Check Digit Verification of cas no

The CAS Registry Mumber 121582-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,5,8 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 121582-52:
(8*1)+(7*2)+(6*1)+(5*5)+(4*8)+(3*2)+(2*5)+(1*2)=103
103 % 10 = 3
So 121582-52-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H16N2O6/c1-20-10-6-4-9(5-7-10)15-16-13(14(19)22-3)11(17)8-12(18)21-2/h4-7,15H,8H2,1-3H3/b16-13-

121582-52-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-[(4-methoxyphenyl)hydrazinylidene]-3-oxopentanedioate

1.2 Other means of identification

Product number -
Other names dimethyl 1-(4-methoxyphenyl)hydrazono-2-oxopropane-1,3-dicarboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:121582-52-3 SDS

121582-52-3Relevant academic research and scientific papers

Synthesis of dimethyl 1-(hetero)aryl-4-oxo-1,4-dihydropyridazine-3,5- dicarboxylates from dimethyl 3-oxopentane-1,5-dioates

Pahovnik, David,Ursic, Uros,Groselj, Uros,Meden, Anton,Svete, Jurij,Stanovnik, Branko

experimental part, p. 407 - 414 (2009/01/31)

Dimethyl 3-oxopentane-1,5-dioate (dimethyl acetone-1,3-dicarboxylate) (1) was transformed first with (hetero)arenediazonium salts 3a-j into dimethyl 2-[(hetero)arylhydrazono]pentane-1,5-dioates 4a - j followed by reaction with N, N-dimethylformamide dimet

Pyridazines with Heteroatom Substituents in Position 3 and 5. 3) 2-Aryl-5-hydroxypyridazin-3(2H)-ones as Potential Herbicides: Synthesis and Some Reactions

Schober, Bernt D.,Megyeri, Gabor,Kappe, Thomas

, p. 169 - 176 (2007/10/02)

The coupling of dimethyl acetonedicarboxylate 1 with a variety of aryldiazonium salts 2a-i produces the hydrazones 3a-i which can be cyclized in boiling dichlorobenzene to yield the pyridazone esters 4a-i, or in sodium hydroxide solution to give the pyrid

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